Literature DB >> 33468642

Rapid Throughput Concentration-Response Analysis of Human Taste Discrimination.

R Kyle Palmer1, Mariah M Stewart2, John Talley2.   

Abstract

Human taste threshold measurements often are used to infer tastant receptor functionality. However, taste thresholds can be influenced by receptor-independent variables. Examination of the full range of taste-active concentrations by taste discrimination has been hampered by logistics of testing multiple concentrations in replicate with human subjects. We developed an automated rapid throughput operant methodology for taste discrimination and applied it to concentration-response analysis of human taste. Tastant solutions (200 µl) drawn from a 96-well plate and self-administered to the tongue served as discriminative stimuli for money-reinforced responses on a touch-sensitive display. Robust concentration-response functions for "basic taste" stimuli were established, with particular focus on agonists of the taste 1 receptor member 2-taste 1 receptor member 3 heterodimer receptor (TAS1R2/R3). With a training cue of 100 mM sucrose, EC50 values of 56, 79, and 310 µM and 40 mM were obtained for rebaudioside A, sucralose, acesulfame potassium, and sucrose, respectively. Changing the sucrose training cue to 300 mM had no impact, but changing to 30 mM resulted in slight leftward shifts in potencies. A signal detection method also was used to determine values of d', a probabilistic value for discriminability, which indicated that 5 mM was near the limits of detection for sucrose. With repeated testing, both EC50 values and 5 mM sucrose d' values were established for each individual subject. The results showed little correspondence between threshold sensitivities and EC50 values for sucrose. We conclude that concentration-response analysis of taste discrimination provides a more reliable means of inferring receptor function than measurement of discriminability at the lowest detectable tastant concentrations. SIGNIFICANCE STATEMENT: Many inferences about human tastant receptor functionality have been made from taste threshold measurements, which can be influenced by variables unrelated to receptors. We herein report a new methodology that enables rigorous concentration-response analysis of human taste discrimination and its use toward quantitative characterization of tastant agonist activity. Our data suggest that taste discrimination concentration-response functions are a more reliable reflection of underlying receptor activity than threshold measures obtained at the lowest detectable tastant concentrations.
Copyright © 2021 The Author(s).

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Year:  2021        PMID: 33468642     DOI: 10.1124/jpet.120.000373

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  3 in total

1.  Why Taste Is Pharmacology.

Authors:  R Kyle Palmer
Journal:  Handb Exp Pharmacol       Date:  2022

2.  A Dynamic Mass Redistribution Assay for the Human Sweet Taste Receptor Uncovers G-Protein Dependent Biased Ligands.

Authors:  Nicole B Servant; Mark E Williams; Paul F Brust; Huixian Tang; Melissa S Wong; Qing Chen; Marketa Lebl-Rinnova; Sara L Adamski-Werner; Catherine Tachdjian; Guy Servant
Journal:  Front Pharmacol       Date:  2022-02-17       Impact factor: 5.810

3.  Human Oral Sensitivity to and Taste Modulation by 3-Mercapto-2-Methylpentan-1-ol.

Authors:  Paul M Wise; Anne Ledyard
Journal:  Chemosens Percept       Date:  2022-02-25       Impact factor: 1.833

  3 in total

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